chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	59491721	59491722	G	A	26	GENIC	homozygous	114206840
5	59492425	59492426	A	G	16	GENIC	homozygous	113821655
5	59493583	59493584	G	A	21	GENIC	homozygous	114206841
5	59496242	59496243	A	G	26	GENIC	homozygous	113821665
5	59497949	59497950	G	A	27	GENIC	homozygous	114206842
5	59498901	59498901		T	21	GENIC	homozygous	128188473
5	59502579	59502580	A	C	23	GENIC	homozygous	114206843
5	59502683	59502684	T	C	29	GENIC	homozygous	113821691
5	59502698	59502699	A	T	30	GENIC	homozygous	113821693
5	59502720	59502721	C	T	31	GENIC	homozygous	114206844
5	59502967	59502968	C	T	29	GENIC	homozygous	114206845
5	59503232	59503233	C	T	17	GENIC	homozygous	113821701
5	59503245	59503246	C	T	18	GENIC	homozygous	113821703
5	59503422	59503423	G	A	33	GENIC	homozygous	114206846
5	59503514	59503515	T	C	27	GENIC	homozygous	113821707
5	59504116	59504117	T	C	23	GENIC	homozygous	113821711
5	59504406	59504407	G	A	23	GENIC	homozygous	114206847
5	59504488	59504489	A	G	30	GENIC	homozygous	113821713
5	59504888	59504889	T	C	26	GENIC	homozygous	113821715
5	59504934	59504935	C	T	25	GENIC	homozygous	114206848
5	59505463	59505464	T	C	16	GENIC	homozygous	113821719
5	59505631	59505632	G	C	17	GENIC	homozygous	114206849
5	59508880	59508881	T	C	18	GENIC	homozygous	114206850
5	59503377	59503380	GAT		29	GENIC	homozygous	132625907